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FDA 510(k)

STIMULATOR, MODEL 7727

K-Number: K782075 · 1978-12-14

ApplicantMedtronic Vascular
Decision Date1978-12-14
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, MODEL 7727 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1978-12-14 under 510(k) number K782075. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, MODEL 7727?

STIMULATOR, MODEL 7727 is a medical device that received FDA 510(k) clearance on 1978-12-14. The listed applicant is Medtronic Vascular. The 510(k) number is K782075.

When did STIMULATOR, MODEL 7727 receive FDA 510(k) clearance?

STIMULATOR, MODEL 7727 received FDA 510(k) clearance on 1978-12-14, under 510(k) number K782075.

Who is the listed applicant for STIMULATOR, MODEL 7727?

The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMULATOR, MODEL 7727?

The FDA product code for STIMULATOR, MODEL 7727 is GZJ.

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Related Devices (Code: GZJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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